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rs281860437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs281860437(-;-)
Make rs281860437(-;TGGAT)
Make rs281860437(TGGAT;TGGAT)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271497
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860437
ebirs281860437
HLIrs281860437
Exacrs281860437
Varsomers281860437
Maprs281860437
PheGenIrs281860437
hapmaprs281860437
1000 genomesrs281860437
hgdprs281860437
ensemblrs281860437
gopubmedrs281860437
geneviewrs281860437
scholarrs281860437
googlers281860437
pharmgkbrs281860437
gwascentralrs281860437
openSNPrs281860437
23andMers281860437
23andMe allrs281860437
SNP Nexus

SNPshotrs281860437
SNPdbers281860437
MSV3drs281860437
GWAS Ctlgrs281860437
Max Magnitude0
ClinVar
Risk rs281860437(TGGAT;TGGAT)
Alt rs281860437(TGGAT;TGGAT)
Reference rs281860437(;)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239274_31239275insATCCA
CLNSRC
CLNACC